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Effect of an Allergen Vaccine in Patients With Allergic Rhino-Conjunctivitis and Asthma Due to House Dust Mite Allergy

Safety, Immunogenicity and Clinical Efficacy of an Allergen Vaccine (AllQbG10) in Subjects With Allergic Rhino-Conjunctivitis and Asthma Due to House Dust Mite Allergy

Status
Completed
Phases
Phase 1Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00652223
Enrollment
21
Registered
2008-04-03
Start date
2005-03-31
Completion date
2005-11-30
Last updated
2008-04-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Allergic Asthma, Perennial Allergic Rhinoconjunctivitis

Brief summary

The purpose of the study is to test the safety, tolerability, immunogenicity and clinical efficacy of the combination treatment AllQbG10 in patients with rhino-conjunctivitis and asthma due to house dust mite allergy in a single-center, open-label setting.

Interventions

BIOLOGICALCYT005-AllQbG10

Immunomodulator CYT003-QbG10 in combination with commercial house dust mite extract as used for routine SIT

Sponsors

Cytos Biotechnology AG
Lead SponsorINDUSTRY

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 55 Years
Healthy volunteers
No

Inclusion criteria

* Mild to moderate perennial allergic rhinoconjunctivitis due to sensitization against house dust mites * Mild asthma * Females only if non-reproductive or agree to practice an effective and accepted method of contraception

Exclusion criteria

* Relevant cardiovascular, renal, pulmonary or endocrine disease * History of autoimmune disease * Severe allergies * History of active infectious disease * Current diagnosis or history of malignancy * Relevant neurological or psychiatric disorder * Pregnancy or lactation * History of alcohol abuse or other recreational drugs * Use of an investigational drug within three month before enrolment * Blood donation within 30 days before enrolment

Countries

Switzerland

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026